Search Ontology:
Human Disease
optic atrophy 6
- Term ID
- DOID:0111435
- Synonyms
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- OPA6
- Definition
- An optic atrophy characterized by early onset of slowly progressive isolated optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 8q21-q22. https://www.ncbi.nlm.nih.gov/pubmed/14508503
- References
- Ontology
- Human Disease ( DOID:0111435 )
- is a type of
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Genes Involved
Zebrafish Models